Canonical Allele Identifier: CA2054318117

Gene: LUM

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91107187_91107189delinsAAG , CM000674.2:g.91107187_91107189delinsAAG	GRCh38
NC_000012.11:g.91500964_91500966delinsAAG , CM000674.1:g.91500964_91500966delinsAAG	GRCh37
NC_000012.10:g.90025095_90025097delinsAAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.5:c.862+929_862+931delinsCTT MANE Select	ENSP00000266718.4:n.862+929_862+931delinsCTT
ENST00000266718.4:c.862+929_862+931delinsCTT	ENSP00000266718.4:n.862+929_862+931delinsCTT
ENST00000546642.1:n.612+929_612+931delinsCTT
ENST00000548071.1:n.255+929_255+931delinsCTT
NM_002345.3:c.862+929_862+931delinsCTT	NP_002336.1:n.862+929_862+931delinsCTT
NM_002345.4:c.862+929_862+931delinsCTT MANE Select	NP_002336.1:n.862+929_862+931delinsCTT